Cargando…
Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations
OBJECTIVES: Human papillomavirus positive (HPV(+)) tonsillar and base of tongue squamous cell carcinoma (TSCC/BOTSCC), the major subsites of oropharyngeal squamous cell carcinoma (OPSCC) have favorable outcome, but upon relapse, outcome is poor and new therapies needed. Since, phosphatidyl-inositol-...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144504/ https://www.ncbi.nlm.nih.gov/pubmed/34046344 http://dx.doi.org/10.3389/fonc.2021.640490 |
_version_ | 1783696972981469184 |
---|---|
author | Holzhauser, Stefan Wild, Nicole Zupancic, Mark Ursu, Ramona G. Bersani, Cinzia Näsman, Anders Kostopoulou, Ourania N. Dalianis, Tina |
author_facet | Holzhauser, Stefan Wild, Nicole Zupancic, Mark Ursu, Ramona G. Bersani, Cinzia Näsman, Anders Kostopoulou, Ourania N. Dalianis, Tina |
author_sort | Holzhauser, Stefan |
collection | PubMed |
description | OBJECTIVES: Human papillomavirus positive (HPV(+)) tonsillar and base of tongue squamous cell carcinoma (TSCC/BOTSCC), the major subsites of oropharyngeal squamous cell carcinoma (OPSCC) have favorable outcome, but upon relapse, outcome is poor and new therapies needed. Since, phosphatidyl-inositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha (PIK3CA) and fibroblast-growth-factor-receptor-3 (FGFR3) mutations often occur in such tumors, here, we tested targeted therapy directed to such genes in TSCC/BOTSCC cell lines. We also combined the two types of inhibitors with each other, and cisplatin or docetaxel that are used clinically. METHODS: The HPV(+) CU-OP-2, -3, -20, UPCI-SCC-154, and HPV(-) CU-OP-17 and UT-SCC-60A cell lines were first tested for common PIK3CA/FGFR3 mutations by competitive-allele-specific TaqMan-PCR. They were then treated with the food and drug administration (FDA) approved drugs, alpelisib (BYL719) and erdafitinib (JNJ-42756493) alone and in combination with cisplatin or docetaxel. Viability, proliferation, apoptosis and cytotoxicity responses were thereafter followed by WST-1 assays and the IncuCyte S3 Live(®) Cell Analysis System. RESULTS: HPV(+) CU-OP-2 had a pS249C-FGFR3, and like CU-OP-20, a pE545K-PIK3CA mutation, while no other lines had such mutations. Irrespectively, dose dependent responses to all PI3K/FGFR inhibitors were obtained, and upon combining the inhibitors, positive effects were observed. Cisplatin and docetaxel also induced dose dependent responses, and upon combination with the inhibitors, both positive and neutral effects were found. CONCLUSIONS: The data suggest that FDA approved drugs alpelisib and erdafitinib efficiently inhibit TSCC/BOTSCC cell line growth, especially when combined irrespective of presence of corresponding mutations and should be further explored, for use upon recurrent disease. |
format | Online Article Text |
id | pubmed-8144504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81445042021-05-26 Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations Holzhauser, Stefan Wild, Nicole Zupancic, Mark Ursu, Ramona G. Bersani, Cinzia Näsman, Anders Kostopoulou, Ourania N. Dalianis, Tina Front Oncol Oncology OBJECTIVES: Human papillomavirus positive (HPV(+)) tonsillar and base of tongue squamous cell carcinoma (TSCC/BOTSCC), the major subsites of oropharyngeal squamous cell carcinoma (OPSCC) have favorable outcome, but upon relapse, outcome is poor and new therapies needed. Since, phosphatidyl-inositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha (PIK3CA) and fibroblast-growth-factor-receptor-3 (FGFR3) mutations often occur in such tumors, here, we tested targeted therapy directed to such genes in TSCC/BOTSCC cell lines. We also combined the two types of inhibitors with each other, and cisplatin or docetaxel that are used clinically. METHODS: The HPV(+) CU-OP-2, -3, -20, UPCI-SCC-154, and HPV(-) CU-OP-17 and UT-SCC-60A cell lines were first tested for common PIK3CA/FGFR3 mutations by competitive-allele-specific TaqMan-PCR. They were then treated with the food and drug administration (FDA) approved drugs, alpelisib (BYL719) and erdafitinib (JNJ-42756493) alone and in combination with cisplatin or docetaxel. Viability, proliferation, apoptosis and cytotoxicity responses were thereafter followed by WST-1 assays and the IncuCyte S3 Live(®) Cell Analysis System. RESULTS: HPV(+) CU-OP-2 had a pS249C-FGFR3, and like CU-OP-20, a pE545K-PIK3CA mutation, while no other lines had such mutations. Irrespectively, dose dependent responses to all PI3K/FGFR inhibitors were obtained, and upon combining the inhibitors, positive effects were observed. Cisplatin and docetaxel also induced dose dependent responses, and upon combination with the inhibitors, both positive and neutral effects were found. CONCLUSIONS: The data suggest that FDA approved drugs alpelisib and erdafitinib efficiently inhibit TSCC/BOTSCC cell line growth, especially when combined irrespective of presence of corresponding mutations and should be further explored, for use upon recurrent disease. Frontiers Media S.A. 2021-05-11 /pmc/articles/PMC8144504/ /pubmed/34046344 http://dx.doi.org/10.3389/fonc.2021.640490 Text en Copyright © 2021 Holzhauser, Wild, Zupancic, Ursu, Bersani, Näsman, Kostopoulou and Dalianis https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Holzhauser, Stefan Wild, Nicole Zupancic, Mark Ursu, Ramona G. Bersani, Cinzia Näsman, Anders Kostopoulou, Ourania N. Dalianis, Tina Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations |
title | Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations |
title_full | Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations |
title_fullStr | Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations |
title_full_unstemmed | Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations |
title_short | Targeted Therapy With PI3K and FGFR Inhibitors on Human Papillomavirus Positive and Negative Tonsillar and Base of Tongue Cancer Lines With and Without Corresponding Mutations |
title_sort | targeted therapy with pi3k and fgfr inhibitors on human papillomavirus positive and negative tonsillar and base of tongue cancer lines with and without corresponding mutations |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144504/ https://www.ncbi.nlm.nih.gov/pubmed/34046344 http://dx.doi.org/10.3389/fonc.2021.640490 |
work_keys_str_mv | AT holzhauserstefan targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations AT wildnicole targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations AT zupancicmark targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations AT ursuramonag targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations AT bersanicinzia targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations AT nasmananders targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations AT kostopoulououranian targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations AT dalianistina targetedtherapywithpi3kandfgfrinhibitorsonhumanpapillomaviruspositiveandnegativetonsillarandbaseoftonguecancerlineswithandwithoutcorrespondingmutations |